Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 25
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs563378859 0.851 0.320 17 7675146 missense variant G/A snv 4.0E-06 2.1E-05 8
rs867114783 17 7675109 missense variant T/C snv 5
rs1555525126 0.925 0.120 17 7673749 missense variant T/C snv 3